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Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency

dc.contributor.authorTÜYSÜZ, Beyhan
dc.contributor.authorDÜNDAR, MUNİS
dc.contributor.authorAghayeva, Asmar
dc.contributor.authorTURAN, Hande
dc.contributor.authorCakir, Aydilek Dagdeviren
dc.contributor.authorGunes, Nilay
dc.contributor.authorEvliyaoglu, Olcay
dc.contributor.authorUyguner, Zehra Oya
dc.contributor.authorToksoy, Guven
dc.contributor.authorBerkay, Ezgi
dc.contributor.authorERCAN, Oya
dc.date.accessioned2021-03-04T10:20:18Z
dc.date.available2021-03-04T10:20:18Z
dc.identifier.citationAghayeva A., TURAN H., Toksoy G., Cakir A. D. , Berkay E., Gunes N., Evliyaoglu O., Uyguner Z. O. , DÜNDAR M., TÜYSÜZ B., et al., "Clinical phenotype and genotype association in patients with 21-hydroxylase deficiency", HORMONE RESEARCH IN PAEDIATRICS, cilt.91, ss.361-362, 2019
dc.identifier.issn1663-2818
dc.identifier.othervv_1032021
dc.identifier.otherav_6cabf525-6449-42ea-9173-27b47db217b1
dc.identifier.urihttp://hdl.handle.net/20.500.12627/75112
dc.language.isoeng
dc.subjectENDOKRİNOLOJİ VE METABOLİZMA
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectPEDİATRİ
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectİç Hastalıkları
dc.subjectEndokrinoloji ve Metabolizma Hastalıkları
dc.titleClinical phenotype and genotype association in patients with 21-hydroxylase deficiency
dc.typeMakale
dc.relation.journalHORMONE RESEARCH IN PAEDIATRICS
dc.contributor.departmentİstanbul Üniversitesi-Cerrahpaşa , ,
dc.identifier.volume91
dc.identifier.startpage361
dc.identifier.endpage362
dc.contributor.firstauthorID267488


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